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Test Code UAD Urinalysis, Diabetic

Additional Codes

Cerner

NextGen

Urinalysis, Diabetic

Urinalysis, Diabetic

UA, Diabetic

 

Useful For

Urinalysis is used to assist in the diagnosis of kidney function, urinary tract infections, carbohydrate metabolism, and liver function. This orderable reflexes to a Microalbumin w/ Creatinine for all specimens that Negative results for Protein U.

Several methods are involved in the analysis of urine specimens:

  • The macroscopic examination of urine includes
    •  The physical appearance, such as color and clarity. 
    • A semiqualitative chemical analysis of the urine is performed by using a multi-parameter test strip that measures pH, protein, glucose, ketones, bilirubin, urobilinogen, nitrite, blood, leukocyte esterase, and specific gravity. These dipstick reactions may be read by visual or instrument methods.
  • Refractometry specific gravity measures the refractive index of a solution with dissolved solids. The index depends on the size and shape of the dissolved molecules.

Methodology

Methodology is dependent on the testing location and specimen specific factors.

  • The UN-3000
    • Siemens Clinitek Novus utilizes dry-pad chemistry technology to measure bilirubin, blood, glucose, ketone, leukocytes, nitrite, pH, protein, urobilinogen, and color. Specific gravity and clarity of urine specimens are determined by measuring the transmission and scattering of light that passes through the specimens.
  • Clinitek Status +
    • An automated semiqualitative chemical analysis of the urine is performed by using a multi-parameter test dip strip that measures pH, protein, glucose, ketones, bilirubin, urobilinogen, nitrite, blood, leukocyte esterase, and specific gravity.
  • Siemens Multistix 10 SG
    • Visual semiqualitative chemical analysis of the urine is performed by using a multi-parameter test dip strip that measures pH, protein, glucose, ketones, bilirubin, urobilinogen, nitrite, blood, leukocyte esterase, and specific gravity.
  • Manual Refractometry

Patient Preparation

None

Collection Instructions

Catheterized specimens collected according to clinical policies and procedures

Radom clean catch instructions: Random Urine Collection Instructions

Specimen Requirements

Preferred Volume

10 mL uncentrifuged and unpreserved, random clean catch or catheterized urine.

Minimum Volume

  • Varies dependent on methodology.
  • All attempts to perform testing will be given based on the volume of specimen received.

Container

  • Sterile/clean plastic urine container

or or

  • Non-preservative urine tube (BD Vacutainer® Ref #364980)

Stability

  • ≤ 2 hours at room temperature
  • ≤ 24 hours refrigerated at 2-8° C if refrigerated within 2 hours of collection

Rejection Criteria

  • Improperly/mislabeled specimens
  • Improperly stored specimens
  • Insufficient specimen volume
  • Specimens collected in preservative tubes

Result Reporting and Reference Values

Reference Range

PROPERTY

REFERENCE RANGE

Color U

Yellow

Clarity U

Clear

pH U

4.5-8.0

Sp Gr U

1.001-1.030

Protein U

Negative

Glu U

Negative

Ketones U

Negative

Bili U

Negative

Nitrite U

Negative

Blood U

Negative

Leuk Est U

Negative

Urobil U

0.2- 1 mg/dL

 

Critical Ranges

None

Reflex Testing

  • A Urinalysis Microscopic will be reflexed when:
    • All patients when the specimen is positive for Leukocytes, Nitrite, and/or Blood
    • Protein
      • ≥1+ Protein if patient is <8 years of age
      • ≥2+ Protein if patient ≥ 8 years of age
  • A Urine Culture will be reflexed when patient is <8 years of age and either of the following occur:
    • Macroscopic is positive for Nitrite and/ or ≥1+ Leukocytes
    • Microscopic shows ≥2+ bacteria and/or > 5 WBC/ HPF
  • A Microalbumin w/ Creatinine will be reflexed for all specimens that have a Negative Protein U result.

Limitations

  • Limitations given for the reagents include specific substances and conditions that may affect the test results. 
  • Because of specimen and reading variability, specimens with analyte concentrations that fall between nominal levels may give results at either level. Results will usually be within one level of the true concentration.
  • As with all laboratory tests, definitive diagnostic or therapeutic decisions should not be based on any single results or method.
  • Color Interferences: Substances that cause abnormal urine color may affect the readability of reagent areas on urinalysis reagent strips.  These substances include visible levels of blood or bilirubin, drugs containing dyes (for example, Pyridium, Azo Gantrisin, Azo Gantanol), nitrofurantoin (Macrodantin, Furadantin), and riboflavin.
  • Protein: 
    • False positive results may be obtained with highly buffered or alkaline urine, or in the presence of quinidine, chlorhexidine, chloroquine, or Lodine (etodolac).
    • The presence of hemoglobin (≥ 5 mg/dL) may cause elevated results.
    • False negative results may occur if curcuma is present.
  • Blood: 
    • Captopril (Capoten) and other compounds containing sulfhydryl groups may reduce the sensitivity. 
    • Certain oxidizing contaminants, such as hypochlorite, may produce false positive results. 
    • Microbial peroxidase associated with urinary tract infection may cause a false positive reaction.
    • False negative results may occur in the presence of acetylcysteine, ascorbic acid, formalin, quinidine, cefoxitin, levodopa, mesna, Keflin, curcuma, Lodine, hydrochlorothiazide, metformin, chlorhexidine, or chloroquine.
  • Leukocytes: 
    • Elevated glucose concentrations (≥3 g/dL) may cause decreased test results. 
    • False negative results may occur in the presence of quinidine, boric acid, Tagamet, glycine, chloroquine, sulfamethoxazole, chlorhexidine, nitrofurantoin, Lodine, hypochlorite,glyburide, or calcium chloride.
    • The presence of cephalexin (Keflex), cephalothin (Keflin), or high concentrations of oxalic acid may also cause decreased test results.Tetracycline may cause decreased reactivity, and high levels of the drug may cause a false negative reaction.
    • Positive results may occasionally be due to contamination of the specimen by vaginal discharge or the presence of formalin or curcuma.
    • High specific gravity may cause falsely low leukocyte results.
  • Nitrite: 
    • A negative result does not rule out significant bacteriuria. 
    • False negative results may occur with shortened bladder incubation of the urine, absence of dietary nitrate, or the presence of nonreductive pathological microbes, ascorbic acid, Lodine, formalin, chlorhexidine, or oxalic acid. 
    • The presence of color precipitates may cause a false positive result.
  • Glucose: 
    • Urine samples with a pH of 9.0 and greater will cause falsely elevated glucose results.
    • False positive results may occur in the presence of hypochlorite, ascorbic acid, captopril, mesna, or curcuma.
    • Ketone bodies reduce the sensitivity of the test. Moderately high ketone levels may cause false negatives for specimens containing small amounts of glucose.
  • Ketone: 
    • False trace results may occur with highly pigmented urine specimens or those containing large amounts of levodopa metabolites. 
    • Compounds that contain sulfhydryl groups, such as mesna (2-mercaptoethane sulfonic acid) and captopril, as well as acetylcysteine, curcuma, formalin, imipenem, or hydrochlorothiazide may cause false positive results or an atypical color reaction.
    • False negative results may occur in the presence of boric acid, formalin, hypochlorite, meropenem, or Lodine.
  • pH: 
    • Bacterial growth by certain organisms in a specimen may cause a marked alkaline shift (pH > 8.0), usually because of urea conversion to ammonia.
  • Bilirubin: 
    • Indican (indoxyl sulfate) can produce a yellow-orange to red color response that may interfere with the interpretation of a negative or positive reading. 
    • Metabolites of etodolac (Lodine) may cause false positive or atypical results.  Atypical colors may indicate the presence of bile pigment abnormalities and the urine specimen should be tested further.
    • The presence of p-aminosalicylic acid, may give a false positive result.
    • A false negative may occur in the presence of acetylcysteine, ascorbic acid, boric acid, hypochlorite, captopril, mesna, nitrite, curcuma, citric acid, chlorhexidine, or oxalic acid.
    • Atypical colors may indicate that bile pigments are present in the urine specimen and may be masking the bilirubin reaction.
  • Urobilinogen: 
    • The reagent area may react with interfering substances known to react with Ehrlick’s reagent, such as ρ-aminosalicylic acid and fulfonamides. 
    • False negative results may be obtained if formalin, acetylcysteine, captropril, hypochlorite, mesna, Tagamet, curcuma, Lodine, sulfamethoxazole,chlorhexidine, glucose, hydrochlorothiazide, lactose, meropenem, or nitrofurantoin is present. 
    • The test is not a reliable method for the detection of porphobilinogen.
  • Specific Gravity: Measurement of specific gravity by refractometry may be influenced by high levels of urinary glucose and protein which can cause underestimation of the actual specific gravity.